drugset / Trial / NCT01599650

Efficacy and Safety of Ranibizumab With or Without Laser in Comparison to Laser in Branch Retinal Vein Occlusion

NCT01599650 ↗

Phase 3 Completed 455 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will generate comparative data for 0.5-mg ranibizumab using PRN dosing administered with or without adjunctive laser treatment versus laser photocoagulation (the current standard of care) up to Month 6 in patients with visual impairment due to ME secondary to BRVO. Additionally the results of this study will provide long-term (24-month) safety and efficacy data for ranibizumab, administered with or without adjunctive laser treatment in this indication.

Timeline

Start
2012-05
Primary completion
2015-05
Completion
2015-05

Outcome

Met primary endpoint

registry 1-ranibizumab Monotherapy vs 3-laser Monotherapy; p <0.0001; difference in LS mean 10.0 (95% CI 7.3 to 12.8); ANOVA NCT01599650 ↗

paper 14.8 and 14.8 vs. 6.0 letters; both P < 0.0001; primary end point met. PMID 27039022 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Ranibizumab Monoclonal antibody 0.5 mg Intravitreal